CEP170B Gene Summary [Human]

Predicted to be located in cytoplasm and microtubule. [provided by Alliance of Genome Resources, Apr 2022]

Details

Type
Protein Coding
Official Symbol
CEP170B
Official Name
centrosomal protein 170B [Source:HGNC Symbol;Acc:HGNC:20362]
Ensembl ID
ENSG00000099814
Bio databases IDs NCBI: 283638 Ensembl: ENSG00000099814
Aliases centrosomal protein 170B, Cep170-related
Synonyms AC124353.1, AI466840, centrosomal protein 170B, CEP170R, FAM68C, KIAA0284, mKIAA0284
Species
Human, Homo sapiens
OrthologiesMouseRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human CEP170B often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • CEP170 C-terminus
  • Inner membrane component of T3SS, cytoplasmic domain
  • FHA domain
  • Forkhead associated domain
  • protein binding
  • zDHHC ankyrin repeat binding domain
  • forkhead associated (FHA) domain superfamily

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • myasthenia gravis
regulated by

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Unknown

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human CEP170B gene, providing context for its role in the cell.

Cellular Component

Where in the cell the gene product is active
  • cytoplasm
  • microtubule

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.